{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86174",
      "recalling_firm": "Conformis, Inc.",
      "address_1": "600 Technology Park Dr",
      "address_2": "N/A",
      "postal_code": "01821-4154",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "NV",
      "recall_number": "Z-2849-2020",
      "product_description": "Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant  Cat: TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT)",
      "product_quantity": "1 kit",
      "reason_for_recall": "Outer box labels for kit 0469247 correct, however the boxes contained the implants and jigs for 0468920",
      "recall_initiation_date": "20200720",
      "center_classification_date": "20200822",
      "termination_date": "20210621",
      "report_date": "20200902",
      "code_info": "Serial Number: 0469247  Exp. 2021-01-31"
    }
  ]
}